P
US7781469B2ExpiredUtilityPatentIndex 49

Arylacetate derivatives having isoxazole skeleton

Assignee: SHIONOGI & COPriority: May 27, 2005Filed: May 23, 2006Granted: Aug 24, 2010
Est. expiryMay 27, 2025(expired)· nominal 20-yr term from priority
Inventors:KANDA YASUHIKO
A61P 9/10A61P 43/00A61P 37/08A61P 3/06A61P 9/12A61P 5/50A61P 5/14A61P 5/16A61P 3/04A61P 25/28A61P 35/00A61P 25/00A61P 29/00A61P 3/10A61P 25/16C07D 417/12A61P 15/08A61P 13/12C07D 413/04C07D 261/08A61P 19/02A61P 17/00A61P 1/18A61P 11/02C07D 413/12A61P 17/06A61P 19/10A61P 1/04
49
PatentIndex Score
1
Cited by
17
References
18
Claims

Abstract

A compound of the formula (I): pharmaceutically acceptable salt or solvate thereof, wherein Y is a group of the formula: wherein Ring A is optionally substituted aryl or optionally substituted heteroaryl, X 3 is COOR 17 or the like Y is not optionally substituted phenyl which is substituted with the formula: —CR 9 R 10 X 3 at the para position, R 1 to R 10 are each independently halogen, hydroxy, optionally substituted lower alkyl, optionally substituted aryl or the like, X 1 is —O—, —S— or the like.

Claims

exact text as granted — not AI-modified
1. A compound of the formula (I): 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof, 
         wherein: 
         Y is a group of the formula: 
       
       
         
           
           
               
               
           
         
         wherein 
         R 5 , R 6 , R 7  and R 8  are each independently hydrogen, halogen, hydroxy, cyano, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted lower alkoxy, optionally substituted lower alkylthio, optionally substituted acyl, optionally substituted amino, optionally substituted aryl, optionally substituted aryloxy, optionally substituted arylthio or optionally substituted heterocycle, 
         R 9  and R 10  are each independently hydrogen, halogen, cyano, optionally substituted lower alkyl, optionally substituted lower alkoxy, optionally substituted amino or optionally substituted aryl, 
         X 3  is COOR 17  or C(═NR 17 )NR 18 OR 19 , 
         wherein R 17 , R 18  and R 19  are each independently hydrogen or optionally substituted lower alkyl, 
         R 1  is optionally substituted aryl or optionally substituted heterocycle, 
         R 2  is optionally substituted lower alkyl, 
         R 3  and R 4  are each independently hydrogen, halogen, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl or optionally substituted heterocycle, and 
         X 1  is O, S or —ON═CR 14 - wherein R 14  is hydrogen or optionally substituted lower alkyl. 
       
     
     
       2. The compound or pharmaceutically acceptable salt thereof according to  claim 1 , wherein R 3  and R 4  are hydrogen. 
     
     
       3. The compound or pharmaceutically acceptable salt thereof according to  claim 1 , wherein R 5 , R 6 , R 7  and R 8  are each independently hydrogen, halogen, optionally substituted lower akyl or optionally substituted lower alkoxy. 
     
     
       4. The compound or pharmaceutically acceptable salt thereof according to  claim 1 , wherein R 9  and R 10  are each independently hydrogen or halogen. 
     
     
       5. The compound or pharmaceutically acceptable salt thereof according to  claim 1 , wherein X 3  is COOR 17  wherein R 17  is hydrogen or optionally substituted lower alkyl. 
     
     
       6. The compound or pharmaceutically acceptable salt thereof according to  claim 1 , wherein R 1  is optionally substituted aryl or heterocycle,
 the substituent(s) of the aryl of R 1  is/are selected from the group consisting of halogen, 
 optionally substituted lower alkyl and optionally substituted lower alkoxy, 
 R 2  is optionally substituted lower alkyl, 
 the substituent(s) of the lower alkyl of R 2  is/are selected from the group consisting of optionally substituted lower alkoxy, lower alkylamino, optionally substituted imino, optionally substituted iminooxy, lower alkylsulfonyl, cycloalkyloxy, optionally substituted aryl and optionally substituted heterocycle, 
 R 3  and R 4  are hydrogen, 
 R 5 , R 6 , R 7  and R 8  are each independently, hydrogen, halogen, lower alkyl or lower alkoxy, 
 R 9  and R 10  are each independently hydrogen or halogen, 
 X 1  is O, S or —ON═CR 14 - wherein R 14  is hydrogen, and 
 X 3  is COOR 17  wherein R 17  is hydrogen or lower alkyl. 
 
     
     
       7. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to  claim 1  as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier. 
     
     
       8. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to  claim 2  as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier. 
     
     
       9. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to  claim 3  as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier. 
     
     
       10. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to  claim 4  as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier. 
     
     
       11. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to  claim 5  as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier. 
     
     
       12. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to  claim 6  as an active ingredient, and a pharmaceutically acceptable excipient and/or carrier. 
     
     
       13. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to  claim 1  to a patient in need thereof. 
     
     
       14. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to  claim 2  to a patient in need thereof. 
     
     
       15. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to  claim 3  to a patient in need thereof. 
     
     
       16. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to  claim 4  to a patient in need thereof. 
     
     
       17. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to  claim 5  to a patient in need thereof. 
     
     
       18. A method of treating hyperlipidemia, obesity, arteriosclerosis, atherosclerosis or hyperglycemia comprising administering an effective amount of the compound or pharmaceutically acceptable salt thereof according to  claim 6  to a patient in need thereof.

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